1 ly a few Atoh1-lineage neurons form a direct spinocerebellar tract.

2 ith terminal dendrites ending in the ventral spinocerebellar tract.

3 generation in the cerebellum, brain stem and spinocerebellar tracts.

4 alamic tract) and proprioception (the dorsal spinocerebellar tract and gracile fasciculus).

5 ing nerves, atrophy of the spinothalamic and spinocerebellar tracts and posterior column-medial lemni

6 e formation of the lateral funiculus and the spinocerebellar tract, and simultaneously perturbing Rob

7 active gliosis in the cerebellum, brainstem, spinocerebellar tracts, and dorsal columns.

8 e activity of a subpopulation of dorsal horn spinocerebellar tract cells by acting through neurokinin

9                                  Dorsal horn spinocerebellar tract cells of adult rats were labelled

10 nt in lamina V and some formed contacts with spinocerebellar tract cells possessing neurokinin-1 rece

11                   Here, we show that ventral spinocerebellar tract neurons (VSCTs) drive generation a

12 ircuitry and physiology of identified dorsal spinocerebellar tract neurons in mouse spinal cord revea

13 ns in the thoraco-lumbar spinal cord: dorsal spinocerebellar tract neurons located in Clarke's column

14 the hindlimbs through several populations of spinocerebellar tract neurons.

15 ception) is relayed to the cerebellum by the spinocerebellar tracts (SCTs).

16  and in the dorsal horn (dhDSCT) and ventral spinocerebellar tract (VSCT) neurons including spinal bo

17 l cell bodies including those of the ventral spinocerebellar tract (VSCT), a tract previously shown t

18      Degeneration of the vestibulospinal and spinocerebellar tracts was mild.